Gene table: search width pubmed_id = 12499478


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency - (AR)
11.10
12499478
CHRND (2q33-q34)
Cholinergic receptor, nicotinic, delta
* Myasthenic syndrome, slow-channel congenital - SCCMS
* Myasthenic syndrome, fast-channel congenital - FCCMS
* Myasthenic syndrome, congenital, 3B, Fast-channel - CMS3B